FDA Inspection 1075109 - MaxiFlex, LLC - December 20, 2018

Record Details

This FDA Inspection record concerns MaxiFlex, LLC, with an inspection on December 20, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: MaxiFlex, LLC
Inspection Date: December 20, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b98fe668-b518-4493-9ea3-6023f480a652